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  • 1980-1984  (5)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 88 (1984), S. 666-668 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 15 (1983), S. 1237-1241 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 15 (1983), S. 915-923 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate coefficient of the reaction \documentclass{article}\pagestyle{empty}\begin{document}$$(2){\rm H}_2 {\rm CN} \to {\rm H} + {\rm HCN}$$\end{document} has been determined in the temperature range of 2700-3500 K using a shock tube technique. C2N2—H2—Ar mixtures were heated behind incident shock waves and the early-time CN history was monitored using broad-band absorption spectroscopy. The rate coefficient providing the best fit to the data was \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm k = (7}{\rm .5}_{ - 2.0}^{{\rm + 2}{\rm .5}} {\rm)} \times {\rm 10}^{{\rm 13}} {\rm cm}^3 /{\rm mol} \cdot {\rm s} $$\end{document} in good agreement with extrapolations of previously published low-temperature results.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 1609-1621 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate coefficient, k, of the reaction \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm H}_2 {\rm O} + {\rm CN} \to {\rm HCN} + {\rm OH} $$\end{document} has been determined in the temperature range 2460-2840 K using a shock tube technique. C2N2—H2O—Ar mixtures were heated behind incident shock waves and the CN and OH concentration time histories were monitored simultaneously using broad-band absorption near 388 nm (CN) and narrow-line laser absorption at 306.67 nm (OH). The rate coefficient expression providing the best fit to the data was \documentclass{article}\pagestyle{empty}\begin{document}$$ k = 2.3{\rm} \times {\rm 10}^{{\rm 13}} \exp (- 6700/T){\rm cm}^3 /{\rm mol s} $$\end{document} with uncertainty limits of about ±45% in the temperature range 2460-2840 K. The rate coefficient of the reverse reaction was calculated using detailed balancing, and its extrapolation to lower temperatures was compared with previously published results.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 231-250 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mixtures of cyanogen and nitrous oxide diluted in argon were shock-heated to measure the rate constants of A broad-band mercury lamp was used to measure CN in absorption at 388 nm [B2Σ+(v = 0) ← X2Σ+(v = 0)], and the spectral coincidence of a CO infrared absorption line [v(2 ← 1), J(37 ← 38)] with a CO laser line [v(6 → 5), J(15 → 16)] was exploited to monitor CO in absorption. The CO measurement established that reaction (3) produces CO in excited vibrational states. A computer fit of the experiments near 2000 K led to \documentclass{article}\pagestyle{empty}\begin{document}$$ k_2 \, = \,10^{11.70\left( { + 0.25, - 0.19} \right)} \,{{{\rm cm}^3 } \mathord{\left/ {\vphantom {{{\rm cm}^3 } {{\rm mol}}}} \right. \kern-\nulldelimiterspace} {{\rm mol}}}\, \cdot \,{\rm s} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_3 \, = \,10^{13.26 \pm 0.26} \,{{{\rm cm}^3 } \mathord{\left/ {\vphantom {{{\rm cm}^3 } {{\rm mol}}}} \right. \kern-\nulldelimiterspace} {{\rm mol}}}\, \cdot \,{\rm s} $$\end{document} An additional measurement of NO via infrared absorption led to an estimate of the ratio k5/k6: with k5/k6 ≃ 103.36±0.27 at 2150 K. Mixtures of cyanogen and oxygen diluted in argon were shock heated to measure the rate constant of and the ratio k5/k6 by monitoring CN in absorption. We found near 2400 K: \documentclass{article}\pagestyle{empty}\begin{document}$$ k_4 \, = \,10^{12.68\left( { + 0.27, - 0.19} \right)} \,{{{\rm cm}^3 } \mathord{\left/ {\vphantom {{{\rm cm}^3 } {{\rm mol}}}} \right. \kern-\nulldelimiterspace} {{\rm mol}}}\, \cdot \,{\rm s} $$\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$$ {{k_5 } \mathord{\left/ {\vphantom {{k_5 } {k_6 }}} \right. \kern-\nulldelimiterspace} {k_6 }}\, = \,10^{2.68 \pm 0.28} $$\end{document} The combined measurements of k5/k6 lead to k5/k6 ≃ 10-3.07 exp(+31,800/T) (±60%) for 2150 ≤ T ≤ 2400 K.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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